EP1583162A2 - Verfahren zur Herstellung eines piezoelektrischen Films, laminierte Struktur aus Substrat und piezoelektrischem Film, piezoelektrischer Aktor und Verfahren zu seiner Herstellung - Google Patents
Verfahren zur Herstellung eines piezoelektrischen Films, laminierte Struktur aus Substrat und piezoelektrischem Film, piezoelektrischer Aktor und Verfahren zu seiner Herstellung Download PDFInfo
- Publication number
- EP1583162A2 EP1583162A2 EP20050006659 EP05006659A EP1583162A2 EP 1583162 A2 EP1583162 A2 EP 1583162A2 EP 20050006659 EP20050006659 EP 20050006659 EP 05006659 A EP05006659 A EP 05006659A EP 1583162 A2 EP1583162 A2 EP 1583162A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- piezoelectric
- film formation
- particles
- substrate
- film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 101
- 238000000034 method Methods 0.000 title claims abstract description 27
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 24
- 239000002245 particle Substances 0.000 claims abstract description 128
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 120
- 239000000443 aerosol Substances 0.000 claims abstract description 63
- 239000000463 material Substances 0.000 claims abstract description 31
- 238000000137 annealing Methods 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 238000010030 laminating Methods 0.000 claims description 3
- 238000003475 lamination Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 230000008021 deposition Effects 0.000 abstract description 2
- 239000010408 film Substances 0.000 description 164
- 239000010410 layer Substances 0.000 description 97
- 239000000428 dust Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000012159 carrier gas Substances 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- 239000004020 conductor Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 239000001307 helium Substances 0.000 description 3
- 229910052734 helium Inorganic materials 0.000 description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 230000007847 structural defect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005489 elastic deformation Effects 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 1
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000011034 rock crystal Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C24/00—Coating starting from inorganic powder
- C23C24/02—Coating starting from inorganic powder by application of pressure only
- C23C24/04—Impact or kinetic deposition of particles
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/07—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base
- H10N30/074—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/20—Piezoelectric or electrostrictive devices with electrical input and mechanical output, e.g. functioning as actuators or vibrators
- H10N30/204—Piezoelectric or electrostrictive devices with electrical input and mechanical output, e.g. functioning as actuators or vibrators using bending displacement, e.g. unimorph, bimorph or multimorph cantilever or membrane benders
- H10N30/2047—Membrane type
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/704—Piezoelectric or electrostrictive devices based on piezoelectric or electrostrictive films or coatings
- H10N30/706—Piezoelectric or electrostrictive devices based on piezoelectric or electrostrictive films or coatings characterised by the underlying bases, e.g. substrates
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/80—Constructional details
- H10N30/85—Piezoelectric or electrostrictive active materials
- H10N30/853—Ceramic compositions
- H10N30/8548—Lead-based oxides
- H10N30/8554—Lead-zirconium titanate [PZT] based
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/42—Piezoelectric device making
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49401—Fluid pattern dispersing device making, e.g., ink jet
Definitions
- the present invention relates to a method for manufacturing a piezoelectric film, to a laminate structure of a substrate and a piezoelectric film, to a piezoelectric actuator, and to a method for manufacturing the same.
- a method called aerosol deposition (AD) is one way to manufacture piezoelectric actuators and the like used in the printer heads of inject printers and so on.
- This method involves dispersing microparticles of a piezoelectric material in gas to produce an aerosol, and ejecting this aerosol toward a substrate surface, and causing the microparticles to collide with and be deposited on the substrate to form a piezoelectric film (see Japanese Patent Application Laid-Open No. 2001-152360 and Japanese Patent Application Laid-Open No. H11-330577, for example).
- the present invention was made in view of the above-mentioned situation, and it is an object thereof to provide a simple method for manufacturing a piezoelectric film that will simultaneously satisfy the various characteristics required thereof.
- the present inventors made the following discoveries upon conducting diligent research aimed at developing a simple method for manufacturing a piezoelectric film that will simultaneously satisfy the various characteristics required thereof.
- Energy possessed by a particle before a collision is not necessarily used for crushing the particle when it collides with the substrate. Only some of the energy may be used for crushing the particle, or almost none of the energy may be used for crushing the particle. If a particle is not crushed by a collision, energy used for crushing the particle is zero. Increase of the number of particles that are not crushed leads to decrease of the average energy used for crushing one particle. Increase of the number of particles that are crushed finer leads to increase of the average energy.
- a film formation is first conducted under conditions in which the average energy is relatively greater, thereby producing a layer with good adhesion, and then a layer with good piezoelectric characteristics is formed on this first layer by forming a film under conditions in which the average energy is relatively smaller.
- This allows the production of a piezoelectric film having a layer with good adhesion on the side facing the substrate, and having a layer with good piezoelectric characteristics on the outside, and makes it possible to achieve both good adhesion to the substrate and good piezoelectric characteristics.
- the present invention was conceived on the basis of these new findings.
- the present invention provides a method for manufacturing a piezoelectric film on a substrate by ejecting an aerosol containing particles of a piezoelectric material onto the substrate so that the particles adhere thereto, comprising:
- the lowering of the average energy in the second film formation step than that in the first film formation step can be accomplished, for example, by lowering the concentration of the particles in the aerosol, by reducing the ejection velocity of the particles within the aerosol, by reducing the angle at which the aerosol is ejected onto the substrate, by changing the size or material of the particles in the aerosol, or by combining these approaches.
- the ejection velocity is preferably set to at least 300 m/sec in the first film formation step, and even more preferably to at least 300 m/sec and not more than 450 m/sec.
- this velocity is preferably at least 150 m/sec and less than 300 m/sec, and even more preferably at least 150 m/sec and not more than 200 m/sec.
- a third piezoelectric layer may be laminated by conducting the ejection such that the average energy is greater than in the second film formation step.
- an annealing treatment in which the piezoelectric film is heated may be performed after completion of all the film formation steps.
- the present invention also provides a method for manufacturing a piezoelectric actuator, in which a piezoelectric film is formed on a conductive substrate constituting one of a pair of positive and negative electrodes, or on a conductive intermediate layer formed on the conductive substrate, by ejecting an aerosol containing particles of a piezoelectric material onto the conductive substrate or the conductive intermediate layer so that the particles adhere thereto, comprising:
- the present invention also provides a laminate structure, comprising a substrate and a piezoelectric film formed by ejecting an aerosol containing particles of a piezoelectric material onto the substrate or an intermediate layer formed over the substrate so that the particles adhere thereto, wherein the piezoelectric film is produced by laminating a plurality of different layers formed by varying average energy used for crushing one of the particles when the particles collide with the substrate or the intermediate layer.
- the layer next to the substrate or the intermediate layer has adhesive strength of at least 20 MPa with the substrate or intermediate layer, has a relative dielectric constant of at least 800, and has a dielectric strength of at least 350 kv/cm.
- the piezoelectric film produced by the lamination of a plurality of layers has adhesive strength of at least 20 MPa with the substrate or the intermediate layer, has a relative dielectric constant of at least 800, and has a dielectric strength of at least 350 kv/cm.
- the present invention can be applied favorably to a piezoelectric actuator used in, e.g., the printer heads of inject printers.
- a conductive material is used for the substrate, this is used as one of the electrodes, and an electrode layer constituting the other electrode is formed on the piezoelectric film.
- a piezoelectric film having a layer with good adhesion on the side facing the substrate, and having a layer with good piezoelectric characteristics on the outside can be produced, and both good adhesion to the substrate and good piezoelectric characteristics can be achieved. Also, since layers having different properties can be laminated by the same AD method merely by varying the film formation conditions, it is possible to obtain a piezoelectric film having good characteristics without a complicated manufacturing process.
- the present invention provides a piezoelectric actuator, comprising a substrate and a piezoelectric film formed on the substrate by ejecting an aerosol containing particles of a piezoelectric material onto the substrate so that the particles adhere thereto, wherein the piezoelectric film comprises a first piezoelectric layer formed on the substrate, and a second piezoelectric layer formed on the first piezoelectric layer, and the particles constituting the first piezoelectric layer are crushed finer than the particles constituting the second piezoelectric layer by conducting the ejection such that average energy used for crushing one of the particles when the particles collide with the substrate in a formation of the first piezoelectric layer is greater than average energy used for crushing one of the particles when the particles collide with the first piezoelectric layer in a formation of the second piezoelectric layer.
- Fig. 1 is a schematic diagram of the film formation apparatus used to form the piezoelectric film of the present invention.
- This film formation apparatus 1 is equipped with an aerosol generator 10 for forming an aerosol 3 by dispersing material particles 2 in a carrier gas, a film formation chamber 20 for ejecting the aerosol 3 from a nozzle and causing the aerosol to adhere to a substrate, and a powder recovery apparatus 30 for recovering the material particles 2 from the aerosol 3 having been used.
- the aerosol generator 10 is equipped with an aerosol chamber 11 capable of accommodating particles 2 of a piezoelectric material in its interior, and a vibrating apparatus 12 that is attached to this aerosol chamber 11 for vibrating the aerosol chamber 11.
- a gas cylinder 13 for introducing a carrier gas is connected to the aerosol chamber 11 via an introduction pipe 14.
- the end of the introduction pipe 14 is located inside and near the bottom of the aerosol chamber 11, and is submerged in the material particles 2.
- the carrier gas include an inert gas such as helium, argon, nitrogen or the like, or the other gas such as air, oxygen or the like.
- the piezoelectric material there are no particular restrictions on the piezoelectric material as long as it is one that is normally used as a material for piezoelectric films. Examples thereof include lead zirconate titanate (PZT), rock crystal, lithium niobate, barium titanate, lead titanate, lead metaniobate, zinc oxide or the like.
- the film formation chamber 20 is equipped with a stage 21 for attaching a substrate 4, and an ejection nozzle 22 provided below this stage 21.
- the ejection nozzle 22 is connected to the aerosol chamber 11 via an aerosol supply pipe 23, and the design is such that the aerosol 3 inside the aerosol chamber 11 is supplied through the aerosol supply pipe 23 to the ejection nozzle 22.
- a drive apparatus (not shown) allows the stage 21 to move in the substrate planar direction with the substrate 4 attached, and the angle of the substrate plane with respect to the direction in which the aerosol is ejected from the ejection nozzle 22 can also be adjusted (see the arrows in the middle of Fig. 1).
- a vacuum pump 25 is connected to this film formation chamber 20 via the powder recovery apparatus 30, allowing the interior of the chamber to be put under reduced pressure.
- the powder recovery apparatus 30 is an electric dust collector, and a plurality of dust filters 32 are disposed in parallel inside a dust trap 31 (see Figs. 2 and 3).
- a dust trap 31 see Figs. 2 and 3.
- the material particles 2 contained in the aerosol are charged by a charger (not shown).
- the dust filters 32 As the aerosol 3 passes through the dust filters 32, the charged particles 2 are adsorbed to the dust filters 32 by electrostatic attraction.
- the carrier gas from which the particles 2 have been removed is exhausted from an exhaust port 34 connected to the vacuum pump 25.
- Each of the dust filters 32 is provided with a scraper 35 capable of moving up and down along the both sides of each filter 32.
- the scrapers 35 When not being used, the scrapers 35 are stowed in scraper holders 36 provided at the top of the dust trap 31.
- a magnet 37A is attached to the upper end of each of the scrapers 35, and magnets 37B corresponding to the magnets 37A on the scraper side are attached to the outer peripheral surfaces of the scraper holders 36.
- the magnets 37B on the side of the scraper holders 36 are capable of moving up and down along the outer peripheral surface of the scraper holders 36. When the scrapers 35 are operated, the magnets 37B of the scraper holders 36 move downward.
- the scrapers 35 are moved downward by the interaction between the magnets 37B of the scraper holders 36 and the magnets 37A of the scrapers 35, and scrape off the particles 2 adhering to the surface of the dust filters 32.
- a hopper 38 is provided at the bottom of the dust filters 32, and the dust that is scraped off falls into this hopper 38 and is recovered.
- the dust filters 32 are generally cleaned by applying an opposite charge in a batch operation, but since the interior of the apparatus here must be kept in a state of reduced pressure, and the flow of the aerosol 3 cannot be stopped, this cleaning is performed with the scrapers 35.
- the material particles 2 are poured into the aerosol chamber 11.
- the carrier gas is then introduced from the gas cylinder 13, and the gas pressure causes the material particles 2 to surge upward.
- the aerosol chamber 11 is vibrated by the vibrating apparatus 12, which mixes the material particles 2 and the carrier gas and generates the aerosol 3.
- the inside of the film formation chamber 20 is reduced in pressure by the vacuum pump 25, and the difference in pressure between the aerosol chamber 11 and the film formation chamber 20 accelerates the aerosol 3 in the aerosol chamber 11 to a high speed and ejects it out of the ejection nozzle 22.
- the material particles 2 contained in the ejected aerosol 3 collide with and deposit on the substrate 4, forming a piezoelectric film.
- the ejection of the aerosol is performed while the substrate 4 is moved in the planar direction by the drive apparatus attached to the stage 21, so that the piezoelectric film is formed over the entire surface of the substrate 4.
- film formation is first performed under conditions in which the average energy used for crushing one particle is relatively greater, creating a first piezoelectric layer 5 with good adhesion (first film formation step), after that, as shown in Fig. 4B, film formation is performed under conditions in which the average energy is relatively smaller, forming on this first layer a second piezoelectric layer 6 with good piezoelectric characteristics (second film formation step).
- first film formation step film formation step
- second film formation step second film formation step
- a two-layer piezoelectric film 7 is formed.
- annealing may be performed if needed, in which the piezoelectric film 7 is heated to at least 500°C for the purpose of restoring the piezoelectric characteristics.
- the average energy for crushing can be adjusted by varying the film formation conditions, such as the particle concentration of the aerosol 3, the collision velocity, or the ejection angle onto the substrate.
- the ejection velocity in the second film formation step may be set to be lower than that in the first film formation step. More specifically, it is preferable for the ejection velocity to be at least 300 m/sec in the first film formation step, and to be at least 150 m/sec and less than 300 m/sec in the second film formation step. It is even more preferable for the ejection velocity to be at least 300 m/sec and not more than 450 m/sec in the first film formation step, and to be at least 150 m/sec and not more than 200 m/sec in the second film formation step.
- the particle concentration in the second film formation step may be set lower than that in the first film formation step.
- the ejection angle in the second film formation step may be set lower than that in the first film formation step.
- the material particles are finely crushed by a greater energy in the first film formation step, causing them to lodge well in the substrate and take on a fine structure, so a layer having a solid grain boundary plane and high adhesion can be produced.
- the energy is relatively low, so the original material particles form a film with fewer structural defects than in the first layer, and some of the material particles are taken into the layer without being crushed, retaining the size they had prior to collision, so a layer can be produced with better piezoelectric characteristics than the first layer.
- the favorable ranges for the other film formation conditions will vary with the other film formation conditions and so forth, and as such cannot be specified unconditionally, but, for example, an excellent piezoelectric film can be formed under conditions in which the pressure inside the film formation chamber is 50 to 400 Pa, the pressure inside the aerosol chamber is 1000 to 80,000 Pa, the nozzle aperture is 10 x 0.4 mm, the carrier gas is helium or air, the nozzle speed relative to the substrate is 1.2 mm/sec, the distance of the nozzle from the substrate is 10 to 20 mm, and the average size of the material particles is 0.3 to 1 ⁇ m.
- a solid layer produced by high energy has good dielectric strength characteristics, and therefore a third piezoelectric layer may be laminated after the second film formation step by ejecting the particles 2 such that the average energy used for crushing one particle will be greater than that in the second film formation step.
- an intermediate layer composed of titanium or other material with good adhesion to the particles may be provided over the substrate, and the material particles may collide with this intermediate layer in the first film formation step. This ensures good layer adhesion even if the collision energy is not so extremely high in the first film formation step.
- the present invention can be applied favorably to piezoelectric actuators used in the printer heads of inject printers and so on.
- a conductive material is used for the substrate, this is used as one of the electrodes, and an electrode layer constituting the other electrode may be formed on the piezoelectric film having been formed.
- FIG. 5 illustrates an embodiment of applying the present invention to a piezoelectric actuator used in an inkjet head.
- An inkjet head 40 comprises a passage unit 43 equipped with a plurality of pressure chambers 42 containing ink 41, and an actuator plate 44 (corresponds to the piezoelectric actuator of the present invention) joined over this passage unit 43 so as to close off the pressure chambers 42.
- the actuator plate 44 comprises a diaphragm 45 (corresponds to the conductive substrate of the present invention) that makes up part of the pressure chambers 42, and a piezoelectric film 46 laminated over the entire surface of this diaphragm 45 on the opposite side from the pressure chambers 42.
- the diaphragm 45 is formed in a rectangular shape and made from stainless steel or other such conductive metal material, and is joined to the top of the passage unit 43 with a thermosetting epoxy adhesive so as to cover the entire top side of the passage unit 43.
- This diaphragm 45 is connected to the ground of a drive circuit IC (not shown), and is also used as a lower electrode.
- the piezoelectric film 46 is formed from zirconate titanate (PZT) or other such ferroelectric piezoelectric ceramic materials, and is laminated in uniform thickness over the entire surface of the diaphragm 45.
- This piezoelectric film 46 is formed by the aerosol deposition method, and comprises two layers: a first piezoelectric layer formed over the diaphragm 45, and a second piezoelectric layer laminated over this first piezoelectric layer.
- An upper electrode 47 (corresponds to the electrode layer of the present invention) is provided on the top side of this piezoelectric film 46, on the opposite side from the side in contact with the diaphragm 45.
- This upper electrode 47 is formed in a specific shape by printing or other such methods from a thin-film conductor, and is connected to a drive circuit IC.
- the piezoelectric film 46 on the diaphragm 45 is subjected to a polarization treatment so as to be polarized in its thickness direction, and when the drive circuit IC causes the potential of the upper electrode 47 to be higher than the potential of the diaphragm 45 (which is the lower electrode), an electric field is applied to the piezoelectric film 46 in the polarization direction (thickness direction) thereof. This causes the piezoelectric film 46 to expand in its thickness direction and contract in its planar direction. As a result, the piezoelectric film 46 and the diaphragm 45 (that is, the actuator plate 44) are locally deformed so as to protrude on the pressure chamber 42 side (unimorph deformation).
- the piezoelectric film 46 is produced by forming a first piezoelectric layer with good adhesion over the diaphragm 45 by performing film formation under conditions of greater particle collision energy, and then forming a second piezoelectric layer with good piezoelectric characteristics over this by performing film formation under conditions of less particle collision energy.
- an intermediate layer may be formed in advance over the diaphragm 45, and the first piezoelectric layer formed over this intermediate layer.
- a sheet of ferritic stainless steel (SUS430 prescribed by Japanese Industrial Standards) with a Vickers hardness Hv of 300 was used as a substrate.
- PZT with a Vickers hardness Hv of 300 to 400 and an average particle size of 0.3 to 1 ⁇ m was used as the material particles.
- a piezoelectric film was formed on the substrate with the sample film formation apparatus as in the embodiment described above. The Vickers hardness of the substrate and the particles was measured with a Nano-Hardness Tester made by +CSM Instruments.
- a first piezoelectric layer was formed on the substrate by ejecting the particles of PZT at a particle velocity of 400 m/sec (first film formation step), and then a second piezoelectric layer was formed on this first piezoelectric layer by ejecting the same at a particle velocity of 170 m/sec (second film formation step). After this, annealing was performed for 1 hour at 600 °C to form a piezoelectric film with a thickness of 10 ⁇ m.
- the other film formation conditions comprised the following: the pressure inside the film formation chamber was 150 Pa, the pressure inside the aerosol was 30000 Pa, the nozzle aperture was 10 x 0.4 mm, the carrier gas was helium, the nozzle speed relative to the substrate was 1.2 mm/sec, and the distance of the nozzle from the substrate was 10 to 20 mm.
- the piezoelectric film thus obtained was measured for dielectric breakdown voltage and P-E hysteresis at room temperature.
- a piezoelectric film was formed in a single film formation step at a particle velocity of 400 m/sec.
- the remaining film formation conditions were the same as in Example 1.
- the piezoelectric film thus obtained was tested in the same manner as in Example 1.
- a piezoelectric film was formed in a single film formation step at a particle velocity of 170 m/sec. The rest of the film formation conditions were the same as in Example 1. The piezoelectric film thus obtained was tested in the same manner as in Example 1.
- Piezoelectric films were formed in a single film formation step by varying the particle velocity between 150 and 450 m/sec. The rest of the film formation conditions were the same as in Example 1. The piezoelectric films thus obtained were tested in the same manner as in Example 1.
- Adhesion was measured by tensile test with a tensile tester. More specifically, in this test, a jig with a cross sectional area of 25 mm 2 was bonded with an epoxy-based adhesive to the surface of the film that had been formed, and this jig was then pulled off.
- Comparative Example 2 in which the particle velocity was 170 m/sec, a film was formed, but its adhesion to the substrate was so weak that the film separated from the substrate when bonded to the film.
- a piezoelectric actuator was produced by forming an upper electrode of 2 x 2 mm by vapor deposition of gold on the piezoelectric film, and using the ferritic stainless steel (SUS430 prescribed by Japanese Industrial Standards) sheet serving as the substrate for the lower electrode.
- the dielectric/piezoelectric characteristics of this piezoelectric actuator were measured and evaluated with a ferroelectric raster.
- Comparative Example 2 in which the particle velocity was 170 m/sec, although a film was formed, separation from the substrate occurred when the upper electrode was formed on the film, so the piezoelectric characteristics could not be evaluated.
- the dielectric breakdown voltage of the piezoelectric actuators discussed above were measured with a trickle current meter and evaluated.
- Example 1 When one layer of piezoelectric film was formed at a particle velocity of 400 m/sec (Comparative Example 1), the dielectric breakdown voltage was 500 kV/cm. In contrast, when two layers of piezoelectric film were formed by varying the particle velocity between 400 m/sec (first film formation step) and 170 m/sec (second film formation step) (Example 1), the dielectric breakdown voltage was 450 kV/cm. Thus, in Example 1, in which a second piezoelectric layer was formed at a lower particle velocity, the dielectric breakdown voltage did decrease slightly, but the dielectric strength characteristics were nearly on a par with those in Comparative Example 1, which comprised just one layer formed at a high particle velocity.
- the adhesion of the particles to the substrate at an ejection velocity of less than 150 m/sec, the particles adhered to the substrate extremely poorly, and the film formation was extremely slow.
- the ejection velocity was at least 150 m/sec, this ensured the minimum energy required for the particles to adhere to the substrate, and a film was formed at a practical rate, but it still took a long time to form a layer of a certain thickness.
- the ejection velocity was at least 300 m/sec, the particles adhered securely to the substrate, or to the particle layer already adhering to the substrate, and a thick layer was formed in a short time.
- the ejection velocity was over 450 m/sec, there was no problem whatsoever with adhesion, but it was confirmed that internal stress in the formed layer resulted in elastic deformation of the substrate.
- the ejection velocity is preferably set to at least 300 m/sec, and that 450 m/sec or less is particularly favorable in order to prevent the layer itself from cracking due to internal stress.
- the ejection velocity is preferably at least 150 m/sec and less than 300 m/sec, and especially at least 150 m/sec and not more than 200 m/sec.
- a piezoelectric film that has good adhesion to the substrate and also has good piezoelectric characteristics and dielectric strength characteristics can be obtained by laminating a first piezoelectric layer formed at a high ejection velocity and a second piezoelectric layer formed at a low ejection velocity.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Particle Formation And Scattering Control In Inkjet Printers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004099006A JP4849432B2 (ja) | 2004-03-30 | 2004-03-30 | 圧電膜の製造方法、基板と圧電膜との積層構造、圧電アクチュエータおよびその製造方法 |
JP2004099006 | 2004-03-30 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1583162A2 true EP1583162A2 (de) | 2005-10-05 |
EP1583162A3 EP1583162A3 (de) | 2006-04-19 |
EP1583162B1 EP1583162B1 (de) | 2009-07-15 |
Family
ID=34879963
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP20050006659 Not-in-force EP1583162B1 (de) | 2004-03-30 | 2005-03-24 | Verfahren zur Herstellung eines piezoelektrischen Films, laminierte Struktur aus Substrat und piezoelektrischem Film, piezoelektrischer Aktor und Verfahren zu seiner Herstellung |
Country Status (5)
Country | Link |
---|---|
US (1) | US7506441B2 (de) |
EP (1) | EP1583162B1 (de) |
JP (1) | JP4849432B2 (de) |
CN (1) | CN100476033C (de) |
DE (1) | DE602005015374D1 (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1968128B1 (de) * | 2007-03-06 | 2010-05-19 | Fujifilm Corporation | Piezoelektrische Vorrichtung, Herstellungsverfahren dafür und Flüssigkeitsentladungsvorrichtung |
WO2018041600A1 (de) * | 2016-08-30 | 2018-03-08 | Siemens Aktiengesellschaft | Verfahren zur aerosoldeposition und verfahren zur herstellung eines keramikteils und vorrichtung zur herstellung von schichten |
EP4191879A1 (de) * | 2021-12-06 | 2023-06-07 | Commissariat à l'énergie atomique et aux énergies alternatives | Verfahren zum übertragen einer schicht |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7633210B2 (en) * | 2003-07-28 | 2009-12-15 | Kyocera Corporation | Multi-layer electronic component and method for manufacturing the same, multi-layer piezoelectric element |
KR100834515B1 (ko) * | 2007-03-07 | 2008-06-02 | 삼성전기주식회사 | 금속 나노입자 에어로졸을 이용한 포토레지스트 적층기판의형성방법, 절연기판의 도금방법, 회로기판의 금속층의표면처리방법 및 적층 세라믹 콘덴서의 제조방법 |
JP2009164312A (ja) | 2007-12-29 | 2009-07-23 | Brother Ind Ltd | 圧電アクチュエータの製造方法及び液体吐出ヘッドの製造方法 |
JP2009184195A (ja) * | 2008-02-05 | 2009-08-20 | Brother Ind Ltd | フィルタの製造方法及び液体移送装置の製造方法 |
JP2010199508A (ja) * | 2009-02-27 | 2010-09-09 | Brother Ind Ltd | 圧電アクチュエータの製造方法、及び、液体移送装置の製造方法 |
AU2010323155B2 (en) * | 2009-11-24 | 2015-12-17 | Kalwar Cft Fusions-Technik Gmbh | Method for surface treating a substrate and device for carrying out the method |
DE102010055042B4 (de) * | 2010-12-17 | 2013-06-06 | Eads Deutschland Gmbh | Verfahren und Vorrichtung zur Bildung eines Elektrolytfilmes auf einer Elektrodenoberfläche |
WO2016007249A1 (en) * | 2014-06-05 | 2016-01-14 | University Of Florida Research Foundation, Inc. | Laterally curved actuators of shape memory materials |
WO2017075344A1 (en) * | 2015-10-28 | 2017-05-04 | Qorvo Us, Inc. | Sensor device with baw resonator and through-substrate fluidic vias |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6013311A (en) * | 1998-06-08 | 2000-01-11 | Eastman Kodak Company | Using morphological changes to make piezoelectric transducers |
EP1046484A2 (de) * | 1999-04-23 | 2000-10-25 | Secretary of Agency of Industrial Science and Technology, Government Agency of Japan | Verfahren zum Herstellen von Gegenständen aus ultrafeinen spröden Pulvern bei niedrigen Temperaturen |
JP2001152360A (ja) * | 1999-11-25 | 2001-06-05 | Ricoh Co Ltd | セラミックス誘電体膜の形成方法、セラミックス誘電体膜/基板の積層構造体、及び電気−機械変換素子 |
EP1231294A1 (de) * | 1999-10-12 | 2002-08-14 | National Institute of Advanced Industrial Science and Technology | Strukturiertes kompositmaterial, herstellungsverfahren und vorrichtung zur herstellung |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2825366B2 (ja) * | 1991-05-23 | 1998-11-18 | 松下電器産業株式会社 | 圧電セラミックス |
US5221870A (en) * | 1991-09-30 | 1993-06-22 | Sumitomo Electric Industries, Ltd. | Surface acoustic wave device |
JP3162584B2 (ja) * | 1994-02-14 | 2001-05-08 | 日本碍子株式会社 | 圧電/電歪膜型素子及びその製造方法 |
KR0157924B1 (ko) * | 1995-12-23 | 1998-12-15 | 문정환 | 데이타 전송 시스템 및 그 방법 |
JPH09184080A (ja) * | 1995-12-27 | 1997-07-15 | Vacuum Metallurgical Co Ltd | 超微粒子による薄膜形成方法、およびその薄膜形成装置 |
US5945293A (en) * | 1997-10-09 | 1999-08-31 | Coulter International Corp. | Protein-colloidal metal-aminodextran coated particle and methods of preparation and use |
JP3308492B2 (ja) | 1998-05-13 | 2002-07-29 | セイコーインスツルメンツ株式会社 | 圧電アクチュエータ |
JP4357659B2 (ja) * | 1998-10-26 | 2009-11-04 | セイコーインスツル株式会社 | 圧電体装置及びその製造方法 |
EP1737054B1 (de) * | 1999-01-29 | 2012-04-11 | Seiko Epson Corporation | Piezoelektrischer Transducer |
US6827634B2 (en) * | 2000-05-22 | 2004-12-07 | Agency Of Industrial Science And Technology | Ultra fine particle film forming method and apparatus |
JP2000328223A (ja) | 1999-05-25 | 2000-11-28 | Agency Of Ind Science & Technol | 積層構造体及びその原料粉、及び、圧電アクチュエータ |
JP2002235181A (ja) * | 1999-10-12 | 2002-08-23 | National Institute Of Advanced Industrial & Technology | 複合構造物及びその製造方法並びに作製装置 |
JP3835960B2 (ja) * | 1999-11-26 | 2006-10-18 | 株式会社リコー | 圧電セラミックス厚膜構造 |
US6801958B2 (en) * | 1999-12-15 | 2004-10-05 | Texas Instruments Incorporated | Method and system for data transfer |
JP3338422B2 (ja) * | 2000-07-06 | 2002-10-28 | 独立行政法人産業技術総合研究所 | 超微粒子材料吹き付け成膜方法 |
US6799200B1 (en) * | 2000-07-18 | 2004-09-28 | International Business Machines Corporaiton | Mechanisms for efficient message passing with copy avoidance in a distributed system |
US6297579B1 (en) * | 2000-11-13 | 2001-10-02 | Sandia National Laboratories | Electron gun controlled smart structure |
JP4118589B2 (ja) * | 2001-04-12 | 2008-07-16 | 独立行政法人産業技術総合研究所 | 樹脂と脆性材料との複合構造物及びその作製方法 |
JP2004085974A (ja) * | 2002-08-28 | 2004-03-18 | Matsushita Electric Ind Co Ltd | 空間光変調器 |
-
2004
- 2004-03-30 JP JP2004099006A patent/JP4849432B2/ja not_active Expired - Lifetime
-
2005
- 2005-03-24 EP EP20050006659 patent/EP1583162B1/de not_active Not-in-force
- 2005-03-24 DE DE200560015374 patent/DE602005015374D1/de active Active
- 2005-03-28 US US11/090,201 patent/US7506441B2/en not_active Expired - Fee Related
- 2005-03-30 CN CNB2005100588442A patent/CN100476033C/zh not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6013311A (en) * | 1998-06-08 | 2000-01-11 | Eastman Kodak Company | Using morphological changes to make piezoelectric transducers |
EP1046484A2 (de) * | 1999-04-23 | 2000-10-25 | Secretary of Agency of Industrial Science and Technology, Government Agency of Japan | Verfahren zum Herstellen von Gegenständen aus ultrafeinen spröden Pulvern bei niedrigen Temperaturen |
EP1231294A1 (de) * | 1999-10-12 | 2002-08-14 | National Institute of Advanced Industrial Science and Technology | Strukturiertes kompositmaterial, herstellungsverfahren und vorrichtung zur herstellung |
JP2001152360A (ja) * | 1999-11-25 | 2001-06-05 | Ricoh Co Ltd | セラミックス誘電体膜の形成方法、セラミックス誘電体膜/基板の積層構造体、及び電気−機械変換素子 |
Non-Patent Citations (5)
Title |
---|
AKEDO J ET AL: "Influence of carrier gas conditions on electrical and optical properties of Pb(Zr,Ti)O3 thin films prepared by aerosol deposition method" JAPANESE JOURNAL OF APPLIED PHYSICS, PART 1 (REGULAR PAPERS, SHORT NOTES & REVIEW PAPERS) JAPAN SOC. APPL. PHYS JAPAN, vol. 40, no. 9B, September 2001 (2001-09), pages 5528-5532, XP002368336 ISSN: 0021-4922 * |
LEBEDEV M ET AL: "Effect of thickness on the piezoelectric properties of lead zirconate titanate films fabricated by aerosol deposition method" JAPANESE JOURNAL OF APPLIED PHYSICS, PART 1 (REGULAR PAPERS, SHORT NOTES & REVIEW PAPERS) JAPAN SOC. APPL. PHYS JAPAN, vol. 41, no. 11b, November 2002 (2002-11), pages 6669-6673, XP002368337 ISSN: 0021-4922 * |
NAKADA M ET AL: "Electro-optical properties of (Pb,La)(Zr,Ti)O3 films prepared by aerosol deposition method" JAPANESE JOURNAL OF APPLIED PHYSICS, PART 1 (REGULAR PAPERS, SHORT NOTES & REVIEW PAPERS) JAPAN SOC. APPL. PHYS JAPAN, vol. 42, no. 9B, September 2003 (2003-09), pages 5960-5962, XP002368338 ISSN: 0021-4922 * |
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 23, 10 February 2001 (2001-02-10) -& JP 2001 152360 A (RICOH CO LTD; NATL INST OF ADVANCED INDUSTRIAL SCIENCE & TECHNOLOGY ME), 5 June 2001 (2001-06-05) * |
TAKAGI K ET AL: "Development of piezoelectric ceramic actuators with graded porosity" MATERIALS SCIENCE FORUM TRANS TECH PUBLICATIONS SWITZERLAND, vol. 423-425, 2003, pages 405-410, XP009062044 ISSN: 0255-5476 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1968128B1 (de) * | 2007-03-06 | 2010-05-19 | Fujifilm Corporation | Piezoelektrische Vorrichtung, Herstellungsverfahren dafür und Flüssigkeitsentladungsvorrichtung |
US8733905B2 (en) | 2007-03-06 | 2014-05-27 | Fujifilm Corporation | Piezoelectric device, process for producing the same, and liquid discharge device |
WO2018041600A1 (de) * | 2016-08-30 | 2018-03-08 | Siemens Aktiengesellschaft | Verfahren zur aerosoldeposition und verfahren zur herstellung eines keramikteils und vorrichtung zur herstellung von schichten |
EP4191879A1 (de) * | 2021-12-06 | 2023-06-07 | Commissariat à l'énergie atomique et aux énergies alternatives | Verfahren zum übertragen einer schicht |
FR3130073A1 (fr) * | 2021-12-06 | 2023-06-09 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Procédé de transfert d’une couche |
Also Published As
Publication number | Publication date |
---|---|
DE602005015374D1 (de) | 2009-08-27 |
US7506441B2 (en) | 2009-03-24 |
EP1583162A3 (de) | 2006-04-19 |
CN100476033C (zh) | 2009-04-08 |
EP1583162B1 (de) | 2009-07-15 |
CN1676667A (zh) | 2005-10-05 |
US20050225208A1 (en) | 2005-10-13 |
JP2005286153A (ja) | 2005-10-13 |
JP4849432B2 (ja) | 2012-01-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7506441B2 (en) | Method for manufacturing a piezoelectric film on a substrate | |
US7054135B2 (en) | Multilayered structure, multilayered structure array and method of manufacturing the same | |
JP3833070B2 (ja) | 液体噴射ヘッドおよび製造方法 | |
US7520596B2 (en) | Method for producing piezoelectric actuator, method for producing ink-jet head, and piezoelectric actuator | |
JP2006203190A (ja) | 無機圧電体のポーリング処理方法、及び、圧電素子の製造方法 | |
EP2056442B1 (de) | Piezoelektrisches aktorelement für einen ultraschallmotor | |
US7268017B2 (en) | Multilayered structure, multilayered structure array and method of manufacturing the same | |
US7771780B2 (en) | Method of producing composite material, method of producing piezoelectric actuator, method of producing ink-jet head, and piezoelectric actuator | |
JP3694652B2 (ja) | 液滴デポジット装置とその製造方法 | |
EP1500509A1 (de) | Flüssigkeitsabgabevorrichtung und Verfahren zur Herstellung derselben | |
JP2006229154A (ja) | 圧電アクチュエータ、インクジェットヘッド、およびそれらの製造方法 | |
JP2008041921A (ja) | 圧電薄膜素子およびその製造方法、ならびにインクジェットヘッドおよびインクジェット式記録装置 | |
JP5121186B2 (ja) | 圧電体、圧電体素子、液体吐出ヘッド及び液体吐出装置 | |
JP2008177353A (ja) | 圧電素子及びインクジェットヘッド | |
JP5131674B2 (ja) | 圧電体とその製造方法、圧電素子とそれを用いた液体吐出ヘッド及び液体吐出装置 | |
WO2010076864A1 (ja) | 圧電素子 | |
WO2010116802A1 (ja) | 圧電素子 | |
JP4094521B2 (ja) | 構造物の製造方法 | |
JP3340043B2 (ja) | 圧電アクチュエータとその製造方法 | |
JP2003309301A (ja) | デバイス製造方法 | |
JP2007335489A (ja) | 圧電体薄膜素子、薄膜アクチュエータ、インクジェットヘッドおよびインクジェット式記録装置 | |
EP1757714A2 (de) | Verfahren zur Herstellung eines Films und eines Tintenstrahldruckkopfes | |
WO2009107552A1 (ja) | インクジェットヘッド及びその駆動方法 | |
JP2004186574A (ja) | 圧電体薄膜素子およびインクジェット記録装置ならびにその製造方法 | |
JP5384843B2 (ja) | 圧電素子構造体の製造方法および圧電素子構造体 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA HR LV MK YU |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA HR LV MK YU |
|
17P | Request for examination filed |
Effective date: 20061009 |
|
AKX | Designation fees paid |
Designated state(s): DE FR GB |
|
17Q | First examination report despatched |
Effective date: 20070202 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: AKEDO, JUN,C/O NATIONAL INSTITUTE OF ADV. INDUST. Inventor name: YASUI, MOTOHIRO,C/O BROTHER KOGYO KABUSHIKI KAISHA |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 602005015374 Country of ref document: DE Date of ref document: 20090827 Kind code of ref document: P |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20100416 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 602005015374 Country of ref document: DE Representative=s name: KUHNEN & WACKER PATENT- UND RECHTSANWALTSBUERO, DE Ref country code: DE Ref legal event code: R081 Ref document number: 602005015374 Country of ref document: DE Owner name: NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIE, JP Free format text: FORMER OWNERS: BROTHER KOGYO K.K., NAGOYA, AICHI, JP; NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY, TOKIO/TOKYO, JP |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E Free format text: REGISTERED BETWEEN 20160211 AND 20160217 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20160315 Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP Owner name: NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIE, JP Effective date: 20160413 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20160323 Year of fee payment: 12 Ref country code: FR Payment date: 20160208 Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602005015374 Country of ref document: DE |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20170324 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20171130 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20170331 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20171003 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20170324 |